1227303-99-2

Basic information

• Product Name: 2-methylene-6-phenylhex-5-yn-1-ol
• Synonyms: 2-methylene-6-phenylhex-5-yn-1-ol
• CAS NO: 1227303-99-2
• Molecular Weight: 186.254
• Mol File: 1227303-99-2.mol

Chemical Properties

• CAS DataBase Reference: 2-methylene-6-phenylhex-5-yn-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylene-6-phenylhex-5-yn-1-ol(1227303-99-2)
• EPA Substance Registry System: 2-methylene-6-phenylhex-5-yn-1-ol(1227303-99-2)

Safety Data

• Hazardous Substances Data: 1227303-99-2(Hazardous Substances Data)

Upstream product

• 1256667-68-1 C₁₃H₁₂O 
• 130602-09-4 6-phenylhex-5-yn-1-al 
• 81302-80-9 2-(trimethylsilylmethyl)prop-2-en-1-ol 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 

Downstream Products

• 1226869-16-4 tert-butyl 2-methylene-6-phenylhex-5-ynyl carbonate 

Relevant articles and documents

Synthesis of Spirocyclic Ethers by Enantioselective Copper-Catalyzed Carboetherification of Alkenols

Spirocyclic ethers can be found in bioactive compounds. This copper-catalyzed enantioselective alkene carboetherification provides 5,5-, 5,6- and 6,6-spirocyclic products containing fully substituted chiral carbon centers with up to 99 % enantiomeric exce

Synthesis of cyclohexene derivatives from 1,5-enynes via gold-catalysis and iodocyclization: A comparative study and applications in the synthesis of 7/5- or 8/5-fused rings and biaryls

A comparative study on the Au(I)-catalyzed and IBr-promoted tandem cyclization of 1,5-enyne was reported. This study provides a meaningful mechanistic insight to the concerted nature of this tandem reaction and also provides interesting applications in the synthesis of 7/5- or 8/5-fused bicycles and biaryls.